2-(4-Methoxyphenyl)-3-methyl-5-prop-1-enyl-1-benzofuran

Details

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Internal ID 5203d3a9-acb2-4117-9f07-80b05d9d7fbc
Taxonomy Phenylpropanoids and polyketides > 2-arylbenzofuran flavonoids
IUPAC Name 2-(4-methoxyphenyl)-3-methyl-5-prop-1-enyl-1-benzofuran
SMILES (Canonical) CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC=C(C=C3)OC
SMILES (Isomeric) CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC=C(C=C3)OC
InChI InChI=1S/C19H18O2/c1-4-5-14-6-11-18-17(12-14)13(2)19(21-18)15-7-9-16(20-3)10-8-15/h4-12H,1-3H3
InChI Key WGNUABUESDBLCY-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H18O2
Molecular Weight 278.30 g/mol
Exact Mass 278.130679813 g/mol
Topological Polar Surface Area (TPSA) 22.40 Ų
XlogP 5.30
Atomic LogP (AlogP) 5.45
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(4-Methoxyphenyl)-3-methyl-5-prop-1-enyl-1-benzofuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7917 79.17%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.6763 67.63%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.9154 91.54%
OATP1B3 inhibitior + 0.9772 97.72%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8591 85.91%
P-glycoprotein inhibitior + 0.8133 81.33%
P-glycoprotein substrate - 0.8278 82.78%
CYP3A4 substrate + 0.5273 52.73%
CYP2C9 substrate - 0.5960 59.60%
CYP2D6 substrate - 0.7145 71.45%
CYP3A4 inhibition - 0.6430 64.30%
CYP2C9 inhibition + 0.7707 77.07%
CYP2C19 inhibition + 0.8912 89.12%
CYP2D6 inhibition - 0.8580 85.80%
CYP1A2 inhibition + 0.9445 94.45%
CYP2C8 inhibition + 0.7803 78.03%
CYP inhibitory promiscuity + 0.9718 97.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8618 86.18%
Carcinogenicity (trinary) Danger 0.5048 50.48%
Eye corrosion - 0.9856 98.56%
Eye irritation - 0.8420 84.20%
Skin irritation - 0.8029 80.29%
Skin corrosion - 0.9783 97.83%
Ames mutagenesis - 0.5954 59.54%
Human Ether-a-go-go-Related Gene inhibition + 0.8779 87.79%
Micronuclear + 0.5659 56.59%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.6773 67.73%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.9307 93.07%
Acute Oral Toxicity (c) III 0.6844 68.44%
Estrogen receptor binding + 0.9645 96.45%
Androgen receptor binding + 0.9025 90.25%
Thyroid receptor binding + 0.8097 80.97%
Glucocorticoid receptor binding + 0.9142 91.42%
Aromatase binding + 0.9187 91.87%
PPAR gamma + 0.8042 80.42%
Honey bee toxicity - 0.8457 84.57%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.7900 79.00%
Fish aquatic toxicity + 0.9787 97.87%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL240 Q12809 HERG 98.04% 89.76%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.30% 91.11%
CHEMBL1907 P15144 Aminopeptidase N 96.11% 93.31%
CHEMBL1951 P21397 Monoamine oxidase A 94.64% 91.49%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.56% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.28% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.90% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.30% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.73% 94.00%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 86.19% 87.67%
CHEMBL3401 O75469 Pregnane X receptor 85.49% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.42% 95.50%
CHEMBL2243 O00519 Anandamide amidohydrolase 84.94% 97.53%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.65% 93.65%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.18% 91.71%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 83.65% 81.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.94% 99.17%
CHEMBL4393 P39900 Matrix metalloproteinase 12 81.52% 92.22%
CHEMBL1907599 P05556 Integrin alpha-4/beta-1 81.24% 92.86%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.14% 86.92%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.59% 93.99%
CHEMBL2581 P07339 Cathepsin D 80.24% 98.95%
CHEMBL3085 P43003 Excitatory amino acid transporter 1 80.15% 94.67%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Krameria bicolor

Cross-Links

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PubChem 72833664
LOTUS LTS0102752
wikiData Q105304640